By Colin Kellaher
Aldeyra Therapeutics has once again filed for Food and Drug Administration of its proposed reproxalap drug candidate for the treatment of signs and symptoms of dry-eye disease.
Aldeyra on Thursday said the resubmission includes results from a recently completed symptom trial the FDA requested late last year when the agency's turned away the Lexington, Mass., company's initial application.
The resubmission also includes a draft label reflecting acute activity in reducing dry-eye symptoms in a dry-eye chamber trial, chronic activity in reducing dry-eye symptoms in a field trial and acute activity in reducing ocular redness in two dry-eye chamber trials.
FDA guidelines call for an acknowledgment of acceptance for review within 30 days of a resubmission and completion of a review within six months.
Write to Colin Kellaher at colin.kellaher@wsj.com
(END) Dow Jones Newswires
October 03, 2024 08:27 ET (12:27 GMT)
Copyright (c) 2024 Dow Jones & Company, Inc.
免责声明:投资有风险,本文并非投资建议,以上内容不应被视为任何金融产品的购买或出售要约、建议或邀请,作者或其他用户的任何相关讨论、评论或帖子也不应被视为此类内容。本文仅供一般参考,不考虑您的个人投资目标、财务状况或需求。TTM对信息的准确性和完整性不承担任何责任或保证,投资者应自行研究并在投资前寻求专业建议。
没有相关数据
如果下载按钮点击无跳转,请点击右上角菜单选择 “在浏览器打开”